Expression of Hemoglobin Variant Migration by Capillary Electrophoresis Relative to Hemoglobin A2Improves Precision
Author(s) -
David F. Keren,
Renee Shalhoub,
Ronald Gulbranson,
Deborah Hedstrom
Publication year - 2012
Publication title -
american journal of clinical pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.859
H-Index - 128
eISSN - 1943-7722
pISSN - 0002-9173
DOI - 10.1309/ajcpof8v0jjopsvf
Subject(s) - hemoglobin , capillary electrophoresis , hemoglobin variants , chromatography , high performance liquid chromatography , coefficient of variation , microbiology and biotechnology , chemistry , hemoglobin a , relative standard deviation , biology , biochemistry , detection limit
We report the precision of the mean migration position of hemoglobin (Hb)S, HbC, HbG (Philadelphia), and HbD (Los Angeles) in 193 samples of whole blood assayed by capillary electrophoresis (CE) and high-performance liquid chromatography (HPLC). By expressing the migration of Hb variants by CE relative to that of HbA(2) in the same sample, there was a significant improvement in the coefficient of variation for each variant studied. The potential usefulness of expressing Hb variants relative to that of HbA(2) was evaluated by comparing the separation of 2 closely migrating Hbs. When expressed by their initial migrations on CE, 25 of the 43 cases of HbG and HbD overlapped. However, when the migrations of these variants were expressed relative to the HbA(2) in the same sample, the 24 cases of HbG separated completely from the 19 cases of HbD. These findings suggest that expressing Hb variants relative to an internal standard, such as HbA(2), may be of value for establishing a library of variant Hbs evaluated by CE.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom